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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55816생성일: 2026년 10월 23일

Triethylamine → Methyl 1-(6-methoxy-3-(trifluoromethyl)quinolin-2-yl)piperidine-4-carboxylate

https://huagongshe.com/ko/reaction/55816

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl isonipecotateHCID 424914—
반응물2-Chloro-6-methoxy-3-(trifluoromethyl)quinolineHCID 86689936—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물Methyl 1-(6-methoxy-3-(trifluoromethyl)quinolin-2-yl)piperidine-4-carboxylateHCID 6698010843%

반응 단계

To a solution of 2-chloro-6-methoxy-3-(trifluoromethyl)quinoline (1.00 g, 3.85 mmol) (see Intermediate 6, Step 8 for synthesis) in IPA (5 mL) was added methyl-4-piperidinecarboxylate (5.50 g, 38.5 mmol) and Et3N (1.17 g, 11.6 mmol). The mixture was heated to reflux for 48 hours. The mixture was diluted with water (100 mL) and extracted with DCM (100 mL×3), the combined organic layers were washed with brine (200 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give the crude product, which was purified by column chromatography on silica gel (PE/EtOAc=15/1) to give the product (600 mg, yield 43%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09433618B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-91f426121a724ce7aa13b19804805233
출처 메모uspto-grants-2016_09